Canonical Allele Identifier: CA545410448

Gene:

Linked Data

• dbSNP Id: rs1287764024
• gnomAD v2: 3-109462515-T-A
• gnomAD v3: 3-109743668-T-A
• gnomAD v4: 3-109743668-T-A
• MyVariant Identifiers: chr3:g.109462515T>A (hg19) ; chr3:g.109743668T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.109743668T>A , CM000665.2:g.109743668T>A	GRCh38
NC_000003.11:g.109462515T>A , CM000665.1:g.109462515T>A	GRCh37
NC_000003.10:g.110945205T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924325.1:n.142+63473T>A